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Indexed/Abstracted in: BIOSIS Previews, Current Contents/Clinical Medicine, EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 1,632
Online ISSN 1827-191X
Dogan R. 1, Faruk Dogan Ö. 1, Öç M. 1, Akata D. 2, Gümüs B. 2, Balkanci F. 2
1 Department of Thoracic and Cardiovascular Surgery Hacettepe University, Ankara, Turkey
2 Department of Radiology Hacettepe University, Ankara-Turkey
The Klippel-Trenaunay sydrome (KTS) is a rare anomaly characterized by naevus, soft tissue hypertrophy and varicosities which is mainly unknown etiology. Associated deep venous system abnormalities have been reported with KTS. Here, a 4-year-old-boy with KTS was reported, because of the associated popliteal vein, common femoral vein with its deep and superficial branches, and external iliac vein agenesis. The originality of the presented case is that we have never observed such a case before.